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1.
嗜热脂肪芽孢杆菌高温蛋白酶的产生条件及酶学性质   总被引:31,自引:0,他引:31       下载免费PDF全文
对嗜热脂肪芽孢杆菌(Bacillusstearothermophilis)WF146的产蛋白酶的条件进行了研究,在58℃条件下,WF146在pH值为75的Fd培养基中振荡发酵培养48h后,发酵液中高温蛋白酶产量可达600u/mL以上。对该酶性质的研究表明,酶分子量为34kD,最适作用pH为80,最适作用温度为80℃,具有良好的pH稳定性及热稳定性。Ca2+对该酶的稳定性具有重要影响,PMSF、DFP及IAA能强烈抑制酶活力,而DTT对该蛋白酶活力无影响  相似文献   

2.
嗜热菌的耐热分子机制   总被引:6,自引:0,他引:6  
对嗜热菌耐热机制在其细胞表层结构、DNA螺旋的热稳定性和嗜热菌酶耐热性等方面的研究作一综述。  相似文献   

3.
以嗜热脂肪芽孢杆菌为材料,通过PolyminP沉淀,硫酸铵分级及Phenyl-Sepharose,DEAE纤维素,磷酸纤维素,FPLC MonoQ,FPLC Superose12等柱层析,得到部分纯化的DNA解链蛋白1。BstH1具有依赖DNA和Mg^2+的ATP酶活力,不同类型的核酸对BstH1的ATP酶活力的促进作用不同。  相似文献   

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用1~#、7~#PPY三种培养基,从保山摆洛塘温泉(86℃,pH7.0)分离到生长温度范围为35—75℃的极端嗜热细菌4株,即“YN8617”、“YN8618”、“YN86290”,YN86291”。经鉴定,“YN3617”和“YN86291”为Bacillus stearother mophilus,“YN86290”为Becillus caldolyticus;“YN3618”暂定为“Extremely thermophilic strains of B.Coagulans”。没有分离到水生栖热菌属(Thermus)的细菌。  相似文献   

6.
以嗜热脂肪芽孢杆菌为材料,通过PolyminP沉淀、硫酸铵分级及DEAE纤维素、磷酸纤维素、Blue-Sepharose、FPLCMonoQ、FPLC Superose12等柱层析,得到了部分纯化DNA解链蛋白BstH2。BstH2具有受DNA促进的ATP酶活力,没类型的核酸对BstH2的ATP酶活力的促进作用没。BstH2在55℃有最高ATP酶活力。这种活力受大肠杆菌单链DNA结合蛋白的抑制及随  相似文献   

7.
从石油污染海域海底泥中筛选到的1株低温石油烃降解菌, 经鉴定为红平红球菌(Rhodococcus erythropolis), 命名为T7-2。该菌株能以十六烷为碳源代谢产生一种对柴油等烃类具良好乳化作用的生物乳化剂。研究表明, 该乳化剂主要由糖类、脂类和蛋白质组成, 其比例为55.43:31.24:12.65。进一步研究证实, 该乳化剂糖类的单糖组成为甘露糖和鼠李糖; 脂类由十碳、十二碳、十六碳及十八碳脂肪酸组成; 蛋白质由16种氨基酸构成。本文还对乳化剂的理化性质进行了分析, 发现它是一种性能稳定、乳化效率高、适应范围较为广泛的生物乳化剂, 对海洋污染生物修复及石油开采都具有潜在的应用价值。  相似文献   

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嗜热脂肪芽孢杆菌HY—69耐热中性蛋白酶的性质研究   总被引:3,自引:0,他引:3  
嗜热脂肪芽孢杆菌HY-69的耐热中性蛋白酶已纯化。研究了纯酶的性质,该酶分子最为24kd,由6个构成一个六聚体。酶的等电点9.15。最适作用pH为7.5,最适作用温度为85℃;该酶具有很好的耐热性,90℃时酶活半寿期为22min,80℃保温3小时,酶活仍保持63%;酶的pH稳定性也好,该酶是金属蛋白酶,活性中心含锌离子,酶的热稳定性依赖于钙离子。测定了酶的氨基酸组成和N末端氨基酸序列。  相似文献   

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A number of thermophilic bacteria capable of utilizing naphthalene as a sole source of carbon were isolated from a high-temperature oilfield in Lithuania. These isolates were able to utilize several other aromatic compounds, such as anthracene, benzene, phenol, benzene-1, 3-diol, protocatechuic acid as well. Thermophilic isolate G27 ascribed to Geobacillus genus was found to have a high aromatic compound degrading capacity. Spectrophotometric determination of enzyme activities in cell-free extracts revealed that the last aromatic ring fission enzyme in naphthalene biotransformation by Geobacillus sp. G27 was inducible via protocatechuate 3, 4-dioxygenase; no protocatechuate 4, 5-dioxygenase, protocatechuate 2, 3-dioxygenase activities were detected. Intermediates such as o-phthalic and protocatechuic acids detected in culture supernatant confirmed that the metabolism of naphthalene by Geobacillus sp. G27 can proceed through protocatechuic acid via ortho-cleavage pathway and thus differs from the pathways known for mesophilic bacteria.  相似文献   

12.
    
The β1,2‐rhamnosyltransferase WsaF is involved in the biosynthesis of a polyrhamnan chain which is attached to the surface‐layer protein from Geobacillus stearothermophilus NRS 2004/3a. The enzyme belongs to the large retaining GT4 family. To date, no structure of a rhamnosyltransferase has been published. Recombinant purified native WsaF has been crystallized, resulting in crystals that belonged to space group P212121 with unit‐cell parameters a = 50.5, b = 56.1, c = 276.8 Å and diffracted to 3.0 Å resolution. Selenomethionine‐variant WsaF crystallized in space group P21 with unit‐cell parameters a = 75.9, b = 75.5, c = 78.1 Å and diffracted to 2.3 Å resolution.  相似文献   

13.
    
The enzyme‐catalysed degradation of starch is central to many industrial processes, including sugar manufacture and first‐generation biofuels. Classical biotechnological platforms involve steam explosion of starch followed by the action of endo‐acting glycoside hydrolases termed α‐amylases and then exo‐acting α‐glucosidases (glucoamylases) to yield glucose, which is subsequently processed. A key enzymatic player in this pipeline is the `Termamyl' class of bacterial α‐amylases and designed/evolved variants thereof. Here, the three‐dimensional structure of one such Termamyl α‐amylase variant based upon the parent Geobacillus stearothermophilusα‐amylase is presented. The structure has been solved at 1.9 Å resolution, revealing the classical three‐domain fold stabilized by Ca2+ and a Ca2+–Na+–Ca2+ triad. As expected, the structure is similar to the G. stearothermophilusα‐amylase but with main‐chain deviations of up to 3 Å in some regions, reflecting both the mutations and differing crystal‐packing environments.  相似文献   

14.
    
Xylanases (1,4‐β‐d ‐xylan xylanhydrolases; EC 3.2.1.8) hydrolyze the 1,4‐β‐d ‐xylopyranosyl linkage of xylans. The detailed structural characterization of these enzymes is of interest for the elucidation of their catalytic mechanism and for their rational modification toward improved stability and specificity. An extracellular xylanase from Geobacillus stearothermophilus T‐6 (XT6) has recently been cloned, overexpressed, purified and biochemically characterized. Previous crystallographic efforts resulted in a hexagonal crystal form, which subsequently proved to be of limited use for structural analysis, mainly because of its relatively poor diffraction quality and resolution. A systematic search for more suitable crystals of XT6 recently resulted in a new crystal form of this enzyme with significantly improved diffraction characteristics. The new crystals belong to a C‐centred monoclinic crystal system (space group C2), with unit‐cell parameters a = 121.5, b = 61.7, c = 89.1 Å, β = 119.7°. These crystals diffract X‐rays to better than 1.5 Å resolution, showing a very clear diffraction pattern of relatively high quality. The crystals are mechanically strong and exhibit excellent radiation‐stability when frozen under cold nitrogen gas. A full diffraction data set to 1.45 Å resolution (94.1% completeness, Rmerge = 7.0%) has been collected from flash‐frozen crystals of the native enzyme at 95 K using synchrotron radiation. Crystals of the E159A/E265A catalytic double mutant of XT6 were found to be isomorphous to those of native XT6. They were used for a full measurement of 1.8 Å resolution diffraction data at 100 K (90.9% completeness; Rmerge = 5.0%). These data are currently being used for the high‐resolution structure determination of XT6 and its mutant for mechanistic interpretations and rational introduction of thermostability.  相似文献   

15.
目的:研究嗜热脂肪土芽孢杆菌CHB1的生长特性与培养条件。方法:以菌体生长量为主要评价指标,利用单因子试验与正交试验相结合的方法对影响CHB1生长的主要因素进行分析。结果:CHB1最低和最高生长温度分别为45℃和74℃,最佳培养温度为60℃;最低和最高起始生长pH值分别为6.5和9.0,最适起始pH为8.0;菌体生长到达对数期的时间为15~18h;接种量2%,装液量40mL,转速180r/min。结论:CHB1为高温菌,生长pH范围偏碱性,条件优化后总菌体浓度可达1.1×109CFU/mL。  相似文献   

16.
The lipase was partially purified by ion exchange chromatography and gel filtration column chromatography, and was characterized from Geobacillus stearothermophilus AH22 strain. The lipase was purified 18.3-folds with 19.7% recovery. The lipase activity was determined by using p-nitrophenyl esters (C2–C12) as substrates. The Km values of the enzyme for these substrates were found as 0.16, 0.02, 0.19 and 0.55?mM, respectively, while Vmax values were 0.52, 1.03, 0.72 and 0.15?U?mg?1. The enzyme showed maximum activity at 50?°C and between pH 8.0 and 9.0. The enzyme was found to be quite stable at pH range of 4.0–10.0, and thermal stability between 50 and 60?°C. It was found that the best inhibitory effect of the enzyme activity was of Hg2+. The inhibitory effect as orlistat, catechin, propyl paraben, p-coumaric acid, 3,4-dihydroxy hydro-cinnamic acid was examined. These results suggest that G. stearothermophilus AH22 lipase presents very suitable properties for industrial applications.  相似文献   

17.
Four novel heat-stable bacteriocin-like substances were found to be produced by Geobacillus stearothermophilus strains isolated from oil-wells in Lithuania. Geobacillus stearothermophilus 32A, 17, 30 and 31 strains were identified as producers of bacteriocins with bactericidal activity against closely related Geobacillus species and several pathogenic strains: Bacillus cereus DSM 12001 and Staphylococcus haemolyticus P903. The secretion of the analysed bacteriocins started during early logarithmic growth and dropped sharply after the culture entered the stationary phase of growth. The antimicrobial activity of the bacteriocins against sensitive indicator cells disappeared after treatment with proteolytic enzymes, indicating their proteinaceous nature. Bacteriocins were stable throughout the pH range between 4 and 10, and no loss in activity was noted following temperature exposures up to 100°C. Direct detection of antibacterial activity on SDS-PAGE suggests that the inhibitory peptides have a molecular weight of 6–7.5 kDa. Such bacteriocins with broad activity spectra, including antipathogenic action, are attractive to the biotechnology industry as they could be used as antimicrobial agents in medicine, agriculture and food products.  相似文献   

18.
A thermophilic facultative bacterial isolate was recovered from 3.2km depth in a gold mine in South Africa. This isolate, designated GE-7, was cultivated from pH 8.0, 50 degrees C water from a dripping fracture near the top of an exploration tunnel. GE-7 grows optimally at 65 degrees C and pH 6.5 on a wide range of carbon substrates including cellobiose, hydrocarbons and lactate. In addition to O(2), GE-7 also utilizes nitrate as an electron acceptor. GE-7 is a long rod-shaped bacterium (4-6microm longx0.5microm wide) with terminal endospores and flagella. Phylogenetic analysis of GE-7 16S rDNA sequence revealed high sequence similarity with G. thermoleovorans DSM 5366(T) (99.6%), however, certain phenotypic characteristics of GE-7 were distinct from this and other previously described strains of G. thermoleovorans.  相似文献   

19.
    
A group I intron that can be spliced in vivo and in vitro was identified in the flagellin gene of the thermophilic bacterium Geobacillus stearothermophilus. We also found one or two intervening sequences (IVS) of flagellin genes in five additional bacterial species. Furthermore, we report the presence of these sequences in two sites of a highly conserved region in the flagellin gene.  相似文献   

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